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相关概念视频

siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

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Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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piRNA - Piwi-interacting RNAs02:57

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PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
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Light Acquisition

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In order to produce glucose, plants need to capture sufficient light energy. Many modern plants have evolved leaves specialized for light acquisition. Leaves can be only millimeters in width or tens of meters wide, depending on the environment. Due to competition for sunlight, evolution has driven the evolution of increasingly larger leaves and taller plants, to avoid shading by their neighbors with contaminant elaboration of root architecture and mechanisms to transport water and nutrients.
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相关实验视频

Updated: Feb 13, 2026

Lineage Labeling of Zebrafish Cells with Laser Uncagable Fluorescein Dextran
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LUCas:光开的Cas13a使用可光分裂的干扰导向RNA.

Carlos F Ng, Deepak Krishnamurthy, Andres Dextre

    bioRxiv : the preprint server for biology
    |February 12, 2026
    PubMed
    概括

    一个新的光激活的CRISPR诊断系统,Light-Uncaged Cas13a (LUCas),精确地控制了Cas13a酶的活性. 这项创新提高了传染病检测的灵敏度,并使多重病毒共感染分析成为可能.

    科学领域:

    • 分子生物学分子生物学
    • 生物技术是生物技术.
    • 诊断检测试验 诊断检测试验

    背景情况:

    • 通过CRISPR诊断,特别是使用Cas13a,通过附带裂变提供灵敏,无放大RNA检测.
    • 限制包括背景酶活性和反应启动的变异性,阻碍了测试灵敏度和解释.
    • 要克服这些挑战,Cas13a需要一个可控制的"启动"机制.

    研究的目的:

    • 开发一种光控制系统,用于精确激活Cas13a,解决CRISPR诊断方面的局限性.
    • 为了提高测试灵敏度,可解释性,并扩大基于Cas13a的检测的设计可能性.
    • 展示使用光门Cas13a的新型多重检测策略.

    主要方法:

    • 介绍光释放的Cas13a (LUCas),使用可光分裂的干扰导向RNA (pc-igRNA) 来关闭Cas13a活动.
    • 紫外线照明释放pc-igRNA抑制,恢复Cas13a的跨裂变活性.
    • 定量运动分析,检测极限预测和验证,以及用于多重检测的时间条码的演示.

    主要成果:

    • 在光激活之前,LUCas显示了大约100倍的Cas13a跨裂变活性抑制.
    • 该系统有效地抑制了目标独立的背景活动,允许预测灵敏度的确定.

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  • 实验验证证证实了预测的检测极限,而时间条码使多重病毒共感染的检测成为可能.
  • 结论:

    • 在诊断应用中,LUCas提供了一个强大的框架,用于基于光的,机械的控制Cas13a活动.
    • 该系统在基于CRISPR的诊断中显著提高了灵敏度和可解释性.
    • LUCas能够实现先进的多重检测策略,扩大了对复杂生物样本的CRISPR诊断的实用性.